RHythmia mAPping and Signal acquisitiOn for Data analYsis (RHAPSODY)

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorBoston Scientific Corporation

About this trial

The objective of the RHAPSODY study is to evaluate the performance of new software features in subjects undergoing standard of care catheter-based endocardial mapping for atrial or ventricular tachyarrhythmias using a commercial Rhythmia Mapping System. Results from this study will be used to guide development and refinement of new software features that may be implemented in future commercial software releases.

Eligibility criteria

Qualifiers

Age 18 or above, or above legal age and willing and capable of giving informed consent specific to national law

Scheduled for standard of care catheter-based endocardial mapping for atrial or ventricular tachyarrhythmias using a commercial Rhythmia Mapping System.

Disqualifiers

Prothrombotic or bleeding tendency due to coagulopathy or blood dyscrasia

Inability to tolerate heparin therapy (e.g. heparin induced thrombocytopenia, allergy, etc.)

Prosthetic or stenotic valves in the chamber where the intended mapping will occur, or in the path of the catheter access route

Active systemic infection or sepsis

Trial design

Treatments tested in this trial

  • Rhythmia Mapping System

Treatment groups

100 Participants
are divided into 1 treatment group

Sponsors and collaborators